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rs33958088

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(CT;CT) 0 common in clinvar
Make rs33958088(A;A)
Make rs33958088(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226937
GeneHBB
is asnp
is mentioned by
dbSNPrs33958088
ebirs33958088
HLIrs33958088
Exacrs33958088
Varsomers33958088
Maprs33958088
PheGenIrs33958088
hapmaprs33958088
1000 genomesrs33958088
hgdprs33958088
ensemblrs33958088
gopubmedrs33958088
geneviewrs33958088
scholarrs33958088
googlers33958088
pharmgkbrs33958088
gwascentralrs33958088
openSNPrs33958088
23andMers33958088
23andMe allrs33958088
SNP Nexus

SNPshotrs33958088
SNPdbers33958088
MSV3drs33958088
GWAS Ctlgrs33958088
Merged fromRs121909828
Max Magnitude0
OMIM141900
Desc
Variant0480
Relatedalso
ClinVar
Risk rs33958088(A,T;A,T)
Alt rs33958088(A,T;A,T)
Reference rs33958088(C;C)
Significance Other
Disease HEMOGLOBIN CHILE
Variation info
Gene HBB
CLNDBN HEMOGLOBIN CHILE
Reversed 1
HGVS NC_000011.9:g.5248167G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016835.2,